Test: | Influenza Virus RNA Detection Supplemental Form if Not Entered into NUlirt– Contact Robbin Williams DHHS |
Synonym: | Flu PCR or rRT-PCR, Influenza Confirmation, FLUPCR, CDC Flu Test |
Method: | Qualitative nucleic acid amplified real time RT-PCR assay |
Availability: | Varies according to testing volume, refer to laboratory for testing interval |
Specimen: | Upper Respiratory Tract: Posterior-pharyngeal swab, nasopharyngeal or nasal swab, nasal aspirate, or nasal wash (1:1 volume with VTM); Lower Respiratory Tract: Tracheal aspirate, bronchoalveolar lavage (BAL), bronchial washes, endotracheal aspirate, endotracheal wash, sputum, lung tissue. (contact the laboratory for guidance if other specimen sources are being considered) |
Collection Device: | Transport human respiratory specimens in Viral Transport Media (VTM) Specimen Labeling: Test subject to CLIA regulations and required 2 patient identifiers on specimen container and requisition forms |
Volume: | Collect 2 - 3 mL from nasopharyngeal wash (using normal saline) or 2 - 3 mL BAL |
Storage/Transport: | Prior to and during shipment: Refrigerated at 2-8° C. Ship within 72h.
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Unacceptable: | Slides, smears; unacceptable sources; Sputum, tracheal aspirates, or throat swabs or samples collected in non-viral transport media or using a bacterial culture swab; dry swabs; wood shaft or calcium alginate swabs; samples collected in EIA or extracted transport media. |
Specimen Stability: | 2-8° C, 72h |
Reference Interval: | Negative |
Reportable Disease: | Positive results (influenza A virus [untypable], influenza B virus [untypable], influenza A virus subtype H3 [seasonal], influenza A virus subtype 2009 [H1N1], influenza B Yamagata lineage or influenza B Victoria lineage) are reported within 7d to local or state health department. Both positive and negative results are reported to the state within 7d for ELR laboratories only. Refer to Nebraska DHHS Title 173, Communicable Diseases. Ship all non-typable influenza A virus specimens to NPHL. |
Comments: | Pre-approval needed from state or local health department. Send approval or notifications to NPHL@unmc.edu or call (402) 559-9444. A false negative result may occur if a specimen is improperly collected, transported or handled. False negative results may also occur if amplification inhibitors are present in the specimen or if inadequate numbers of organisms are present in the specimen. |
Revised: | 12/4/2020 |